VT-3989 is under clinical development by Vivace Therapeutics and currently in Phase II for Solid Tumor. According to GlobalData, Phase II drugs for Solid Tumor have a 38% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how VT-3989’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.
GlobalData tracks drug-specific phase transition and likelihood of approval scores, in addition to indication benchmarks based off 18 years of historical drug development data. Attributes of the drug, company and its clinical trials play a fundamental role in drug-specific PTSR and likelihood of approval.
VT-3989 overview
VT-3989 is under development for the treatment of relapsed and refractory NF2 mutated malignant pleural mesothelioma and solid tumors. It is administered through the oral route as a capsule. The drug candidate acts by targeting Hippo-Yap pathway and yes-associated protein (YAP) and transcriptional enhanced associate domain (TEAD).
Vivace Therapeutics overview
Vivace Therapeutics is an oncology-focused small molecule drug discovery and development company. The company develops multiple novel small-molecule medicines targeting the Hippo-YAP pathway, which is involved in the regulation of cell proliferation, programmed cell death and cell migration. Vivace Therapeutics is headquartered in San Mateo, California, the US.
For a complete picture of VT-3989’s drug-specific PTSR and LoA scores, buy the report here.
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